A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328679



Internal ID22285633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11609196..11609365hg38UCSC Ensembl
chr1:11669253..11669422hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200031
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328679
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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